© 2001 Journal of Clinical Pathology
Reduced expression of
-catenin, ß-catenin, and
-catenin is associated with high cell proliferative activity and poor differentiation in non-small cell lung cancer
1 Departments of Pathology and Forensic Medicine, University of Kuopio and Kuopio University Hospital, PO Box 1627, FIN-70211 Kuopio, Finland
2 Department of Pathology, Centre for Laboratory Medicine, Tampere University Hospital, PO Box 2000, FIN-33521 Tampere, Finland
3 Department of Oncology, University of Kuopio and Kuopio University Hospital
4 Department of Pathology, Satakunta Central Hospital, FIN-28500 Pori, Finland
Correspondence to:
Dr Kosma Velimatti.Kosma{at}uku.fi
AimsTo investigate the expression of catenins (
, ß, and
) in non-small cell lung carcinoma (NSCLC) and its relation to clinicopathological factors and prognosis.
MethodsThe expression of catenins was analysed immunohistochemically in 261 patients with resected NSCLC, diagnosed between 1978 and 1996 in eastern Finland. The cell proliferation index of the tumours was analysed by means of an image analyser. The staining results were compared with clinicopathological characteristics and survival.
ResultsNormal catenin staining was found significantly more often in adenocarcinomas than in squamous cell carcinomas or anaplastic/large cell carcinomas. Reduced staining of
-catenin, ß-catenin, and
-catenin was related to poor differentiation of the tumour. The tumours with reduced staining of ß-catenin or
-catenin often had higher cell proliferation activity. Nuclear staining of ß-catenin and
-catenin was found in 16 (7%) and 29 (13%) cases, respectively. This nuclear staining correlated directly with increased cell proliferation and inversely with membranous staining. In survival analyses the predictors of overall and disease free survival were stage and tumour type. The expression of catenins did not affect survival.
ConclusionsThe expression of
-catenin, ß-catenin, and
-catenin is related to histological type and differentiation in NSCLC, although catenins have no independent prognostic value. However, this study supports the important role of the nuclear accumulation of ß-catenin and
-catenin in highly proliferative cells.
Key Words: catenin lung cancer proliferation differentiation
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
-
Leinonen, T, Pirinen, R, Bohm, J, Johansson, R, Rinne, A, Weber, E, Kosma, V-M
(2007). Biological and prognostic role of acid cysteine proteinase inhibitor (ACPI, cystatin A) in non-small-cell lung cancer. J. Clin. Pathol.
60: 515-519
[Abstract] [Full Text] -
Shen, J., Behrens, C., Wistuba, I. I., Feng, L., Lee, J. J., Hong, W. K., Lotan, R.
(2006). Identification and Validation of Differences in Protein Levels in Normal, Premalignant, and Malignant Lung Cells and Tissues Using High-Throughput Western Array and Immunohistochemistry. Cancer Res.
66: 11194-11206
[Abstract] [Full Text] -
Gastaldi, T., Bonvini, P., Sartori, F., Marrone, A., Iolascon, A., Rosolen, A.
(2006). Plakoglobin is differentially expressed in alveolar and embryonal rhabdomyosarcoma and is regulated by DNA methylation and histone acetylation. Carcinogenesis
27: 1758-1767
[Abstract] [Full Text] -
Zhu, C-Q, Shih, W, Ling, C-H, Tsao, M-S
(2006). Immunohistochemical markers of prognosis in non-small cell lung cancer: a review and proposal for a multiphase approach to marker evaluation.. J. Clin. Pathol.
59: 790-800
[Abstract] [Full Text] -
Huang, C.-l., Liu, D., Nakano, J., Ishikawa, S., Kontani, K., Yokomise, H., Ueno, M.
(2005). Wnt5a Expression Is Associated With the Tumor Proliferation and the Stromal Vascular Endothelial Growth Factor--An Expression in Non-Small-Cell Lung Cancer. JCO
23: 8765-8773
[Abstract] [Full Text] -
Ramburan, A, Oladiran, F, Smith, C, Hadley, G P, Govender, D
(2005). Microsatellite analysis of the adenomatous polyposis coli (APC) gene and immunoexpression of {beta} catenin in nephroblastoma: a study including 83 cases treated with preoperative chemotherapy. J. Clin. Pathol.
58: 44-50
[Abstract] [Full Text] -
Winn, R. A., Heasley, L. E.
(2004). {gamma}-Catenin Expression Is Reduced or Absent in a Subset of Human Non-small Cell Lung Cancers, and Its Re-expression Inhibits Cell Growth. Chest
125: 122S-123S
[Full Text] -
Choi, Y. S., Shim, Y. M., Kim, S.-H., Son, D. S., Lee, H.-S., Kim, G. Y., Han, J., Kim, J.
(2003). Prognostic significance of E-cadherin and {beta}-catenin in resected stage I non-small cell lung cancer. Eur. J. Cardiothorac. Surg.
24: 441-449
[Abstract] [Full Text] -
Kotsinas, A., Evangelou, K., Zacharatos, P., Kittas, C., Gorgoulis, V. G.
(2002). Proliferation, but Not Apoptosis, Is Associated with Distinct {beta}-Catenin Expression Patterns in Non-Small-Cell Lung Carcinomas : Relationship with Adenomatous Polyposis Coli and G1-to S-Phase Cell-Cycle Regulators. Am. J. Pathol.
161: 1619-1634
[Abstract] [Full Text] -
Shtutman, M., Zhurinsky, J., Oren, M., Levina, E., Ben-Ze'ev, A.
(2002). PML Is a Target Gene of {beta}-Catenin and Plakoglobin, and Coactivates {beta}-Catenin-mediated Transcription. Cancer Res.
62: 5947-5954
[Abstract] [Full Text] -
Kofron, M., Heasman, J., Lang, S. A., Wylie, C. C.
(2002). Plakoglobin is required for maintenance of the cortical actin skeleton in early Xenopus embryos and for cdc42-mediated wound healing. JCB
158: 695-708
[Abstract] [Full Text] -
Bremnes, R. M., Veve, R., Gabrielson, E., Hirsch, F. R., Baron, A., Bemis, L., Gemmill, R. M., Drabkin, H. A., Franklin, W. A.
(2002). High-Throughput Tissue Microarray Analysis Used to Evaluate Biology and Prognostic Significance of the E-Cadherin Pathway in Non-Small-Cell Lung Cancer. JCO
20: 2417-2428
[Abstract] [Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
